| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:45215970-45216382 | Common:2; Rare:137 | ||||
| chr12:45990425-45990989 | Common:3; Rare:176 | ||||
| chr12:45991973-45992204 | Common:2; Rare:52 | ||||
| chr12:46267353-46267398 | Rare:10 | ||||
| chr12:46268578-46269304 | Common:2; Rare:182 | ||||
| chr12:46269308-46269450 | Rare:34 | ||||
| chr12:46269950-46270132 | Common:1; Rare:34 | ||||
| chr12:46371341-46371562 | Common:2; Rare:97 | ||||
| chr12:46372638-46373065 | Common:1; Rare:161 | ||||
| chr12:47705951-47706130 | Rare:74 | ||||
| chr12:47963474-47963668 | Common:1; Rare:53 | ||||
| chr12:48105791-48105948 | Common:1; Rare:38 | ||||
| chr12:48105971-48106222 | Common:2; Rare:83 | ||||
| chr12:48106276-48106419 | Rare:43 | ||||
| chr12:48119181-48119398 | Common:2; Rare:43; Clinvar:4; Clinvar (benign):2 |